Relu Cloud
K-Number: K252708 · 2026-04-10
ApplicantRelu BV
Decision Date2026-04-10
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Relu Cloud is a medical device manufactured by Relu BV. It received FDA 510(k) clearance on 2026-04-10 under approval number K252708. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Relu Cloud?
Relu Cloud is a medical device that received FDA 510(k) clearance on 2026-04-10. It is manufactured by Relu BV. The 510(k) number is K252708.
When was Relu Cloud approved by the FDA?
Relu Cloud received FDA 510(k) clearance on 2026-04-10, under approval number K252708.
What company makes Relu Cloud?
Relu Cloud is manufactured by Relu BV.
What is the FDA product code for Relu Cloud?
The FDA product code for Relu Cloud is QIH.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.